Quality Document Control Specialist

Hybrid: After training in Novato, CA Duties: The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP-controlled documentation system and for providing the various departments the documentation that is necessary to perform cGxP activities. Other responsibilities include auditing existing documentation, reporting document...

Job DescriptionJob DescriptionHybrid: After training in Novato, CADuties:The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP-controlled documentation system and for providing the various departments the documentation that is necessary to perform cGxP activities.Other responsibilities include auditing existing...

QA Document Control Specialist (Part Time)Location: Novato, CA (Hybrid)Pay Rate: $34/hr.7 month assignment (Strong potential to extend or convert to FTE)Our client, a global leader in biotechnology and innovation of therapies for rare and genetic diseases and life-threatening conditions is seeking a QA Documentation Control Specialist II that will be...

QA Document Control Specialist (Part Time)Location: Novato, CA (Hybrid)Pay Rate: $34/hr.7 month assignment (Strong potential to extend or convert to FTE)Our client, a global leader in biotechnology and innovation of therapies for rare and genetic diseases and life-threatening conditions is seeking a QA Documentation Control Specialist II that will be...

QC Analyst Location: Novato, CA. (On-Site) 12-month assignment (potential to extend or convert) Pay Rate: $28/hr. Schedule: Morning Shift Our pharmaceutical industry client, a global leader in therapeutics for rare and life-threatening genetic diseases, is looking for a QC Analyst that will primarily focus on the centralized program management of reference...

QC Analyst Location: Novato, CA. (On-Site) 12-month assignment (potential to extend or convert) Pay Rate: $28/hr. Schedule: Morning Shift Our pharmaceutical industry client, a global leader in therapeutics for rare and life-threatening genetic diseases, is looking for a QC Analyst that will primarily focus on the centralized program management of reference...

QC Analyst Location: Novato, CA. (On-Site) 12-month assignment (potential to extend or convert) Pay Rate: $28/hr. Schedule: Morning Shift Our pharmaceutical industry client, a global leader in therapeutics for rare and life-threatening genetic diseases, is looking for a QC Analyst that will primarily focus on the centralized program management of reference...

Job ID: 24-01475 Technical Manager, Quality Systems Description *** is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These...

Title: Technical Manager, Quality Systems Location: Novato, CA Duration: 9+ months Description The company is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of...

Technical Manager, Quality Systems Description *** is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often...

Quality Systems Technical Manager Location: Novato, CA 9-month assignment (potential to extend) Pay Rate: $50-60/hour Our leading pharmaceutical client is looking for a global leader in developing therapeutics for patients with serious and life-threatening rare genetic diseases. Summary Description: The Quality Systems Technical Manager plays a vital role in...

Job DescriptionJob DescriptionDescriptionThe Company is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases.We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children.These conditions are often...

Job DescriptionJob DescriptionBiotechnology company is hiring a Quality Technical Manager to ensure the company's Quality Systems, such as Documentation, Deviation, CAPA, Change Control, Self-Inspection and Risk Management are consistently administered and followed. ResponsibilitiesParticipate in inspection readiness, regulatory inspection support and...

Innova Solutions is immediately hiring for Specialist, QA OperationsPosition type: Full time ContractDuration: 13+ Months Location: Novato, CAAs a Specialist, QA Operations you will: DescriptionPrimary Responsibilities: Provide quality oversight of one or more portions of operations including, but not limited to; Direct observation of manufacturing operation...

Our client develops and publishes some of the most popular video game franchises on the planet. The IT and Security teams build, monitor, and maintain their corporate and production infrastructure that their fans need to play their games. They are experts in systems, networks, cloud technology and security. Their teams maintain the enterprise and development...

**About DNI Group LLC** DNI provides the food industry with innovative Japanese seafood products, sashimi grade seafood, authentic Japanese inspired appetizers, unique desserts, and plant-based seafood options. Our value proposition is to continually provide quality brands, accurate service, reliable inventory, and on-time delivery to our customers. **The...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...